Associated Papers
Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly.
Uctepe E et al.
European Journal of Human Genetics : Ejhg, 2024
Genetics of recessive cognitive disorders.
Musante L et al.
Trends in Genetics : Tig, 2014
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Najmabadi H et al.
Nature, 2011
Select a paper to view details